A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515916



Internal ID15442973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57434294..61107733hg38UCSC Ensembl
Innerchr6:57299092..58075480hg19UCSC Ensembl
Innerchr6:57407051..58183439hg18UCSC Ensembl
Innerchr6:57407051..58183439hg17UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg383673440
hg19776389
hg18776389
hg17776389
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688375, nssv697427, nssv685995, nssv695417, nssv674856, nssv665299, nssv695845
Samples
Known GenesPRIM2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515916
Frequency
Sample Size2026
Observed Gain5
Observed Loss2
Observed Complex0
Frequencyn/a


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